首页> 外文期刊>Journal of Inorganic Biochemistry: An Interdisciplinary Journal >Metal complexes of carboxamidrazone analogs as antitubercular agents - 1. Synthesis, X-ray crystal-structures, spectroscopic properties and antimycobacterial activity against Mycobacterium tuberculosis H(37)Rv
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Metal complexes of carboxamidrazone analogs as antitubercular agents - 1. Synthesis, X-ray crystal-structures, spectroscopic properties and antimycobacterial activity against Mycobacterium tuberculosis H(37)Rv

机译:羧酰胺dra类似物的金属配合物作为抗结核药-1.合成,X射线晶体结构,光谱性质和对结核分枝杆菌H(37)Rv的抗分枝杆菌活性

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摘要

N-1-Benzylidene-pyridine carboxamidrazones and their metal conjugates have emerged as a new class of potential antimycobacterial agents. Nine such carboxamidrazone analogs (L-1-L-9) along with their Cu(II) (MC1-MC9) and Fe(III) (MC10-MC18) complexes were synthesized. Single crystal X-ray structures of copper complexes MC1 and MC5 were determined which suggest slightly distorted square planer geometries for copper complexes and octahedral geometries for ferric compounds. All compounds were evaluated for their in vitro antimycobacterial activity against Mycobacterium tuberculosis H(37)Rv. The results show 32-64-fold enhancement in antitubercular activity upon copper complexation.
机译:N-1-苄叉吡啶吡啶甲酰胺dra及其金属结合物已成为一类潜在的抗分枝杆菌药物。合成了九个这样的羧ami龙类似物(L-1-L-9)以及它们的Cu(II)(MC1-MC9)和Fe(III)(MC10-MC18)复合物。确定了铜配合物MC1和MC5的单晶X射线结构,这表明铜配合物的正方形平面几何形状略有扭曲,铁化合物的八面体几何形状则略有扭曲。评价所有化合物对结核分枝杆菌H(37)Rv的体外抗分枝杆菌活性。结果表明铜络合后抗结核活性提高了32-64倍。

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